Canonical Allele Identifier: CA121912033

Gene: RPS23 ATG10

Linked Data

• dbSNP Id: rs925894154
• gnomAD v4: 5-82276716-T-C
• MyVariant Identifiers: chr5:g.81572535T>C (hg19) ; chr5:g.82276716T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82276716T>C , CM000667.2:g.82276716T>C	GRCh38
NC_000005.9:g.81572535T>C , CM000667.1:g.81572535T>C	GRCh37
NC_000005.8:g.81608291T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296674.13:c.165-198A>G (RPS23) MANE Select	ENSP00000296674.8:n.165-198A>G
ENST00000651545.1:c.165-198A>G (RPS23)	ENSP00000498621.1:n.165-198A>G
ENST00000296674.12:c.165-198A>G (RPS23)	ENSP00000296674.8:n.165-198A>G
ENST00000503605.1:n.374-198A>G (RPS23)
ENST00000504293.5:n.260-198A>G (RPS23)
ENST00000507980.1:c.165-198A>G (RPS23)	ENSP00000422071.1:n.165-198A>G
ENST00000510019.5:c.165-198A>G (RPS23)	ENSP00000425833.1:n.165-198A>G
ENST00000510210.5:c.165-198A>G (RPS23)	ENSP00000427043.1:n.165-198A>G
ENST00000512493.5:c.165-198A>G (RPS23)	ENSP00000425865.1:n.165-198A>G
ENST00000514253.2:n.763T>C (ATG10)
NM_001025.4:c.165-198A>G (RPS23)	NP_001016.1:n.165-198A>G
NM_001025.5:c.165-198A>G (RPS23) MANE Select	NP_001016.1:n.165-198A>G